Liquid detergent compositions having good foaming and grease emulsification properties as well as reduced skin irritation effects which consist essentially of, by weight, 8% to 30% of a water-soluble C10 --C16 alkyl ether ethylenoxy sulfate salt containing an average of 5 to 12 moles of ethylene oxide in the molecule, a supplementary, water-soluble, non-soap, anionic detergent having in its molecular structure a C8 --C22 alkyl alkenyl or acyl group, and a sulfonate, sulfate or carboxylate group, the weight ratio of said alkyl ether sulfate to said supplementary detergent being in the range of 1:1 to 20:1; 1% to 8% of a zwitterionic detergent having the structural formula ##STR1## wherein R is a C8 --C18 alkyl or C8 --C18 alkanamido C2 --C3 alkyl group, R1 is a C1 --C3 alkyl, R2 is a C1 --C4 alkylene or hydroxyalkylene and X is S:O or C; 1% to 8% of an N--C8 --C18 alkonoic acid C2 --C3 alkanolamide, the weight ratio of said alkanolamide to said zwitterionic detergent being in the range of 1:4 to 4:1; and the balance being an aqueous medium comprising water and from 2% to 20% of a solubilizer selected from the group consisting of C2 --C3 alcohols, hydrotropes and mixtures thereof. Preferred compositions include, in addition, 2% to 10% by weight of an anti-gelling agent, such as a water-soluble formate. These compositions are characterized by good foaming, cleaning and skin mildness characteristics and are suitable for use as shampoos, dishwashing liquids, liquid soaps and foam baths.

Patent
   4554098
Priority
Feb 19 1982
Filed
Feb 19 1982
Issued
Nov 19 1985
Expiry
Nov 19 2002
Assg.orig
Entity
Large
40
12
all paid
1. A high foaming, liquid detergent composition having reduced skin-irritation properties which consists essentially of, by weight, 12% to 24% of alkyl ether sulfate having the structural formula
R(OC(2)H(4))nOSO(3)M
wherein R is an alkyl of 10 to 16 carbon atoms, n has an average value of 5 to 12 and M is a cation; a supplementary, water-soluble, non-soap, anionic detergent having in its molecular structure a C(7)--C(22) alkyl, alkenyl or acyl group and a sulfonate, sulfate or carboxylate group, the weight ratio of said alkyl ether sulfate to said supplementary detergent being in the range of 1.5:1 to 6:1; 2% to 6% of a zwitterionic detergent having the structural formula ##STR5## wherein R is C(8)--C(18) alkyl or C(8)--C(18) alkanamido C(2)--C(3) alkyl group, R1 is a C(1)--C(4) alkylene or hydroxylene group; 2% to 6% of an N-C(12)--C(14) alkanoic acid C(2)--C(3) alkanolamide, the weight ratio of said alkanolamide to said zwitterionic detergent being in the range of 1:2 to 2:1; and the balance being an aqueous medium containing 2% to 20% of a solubilizer.
2. A detergent composition according to claim 1 wherein said solubilizer is selected from the group consisting of C2 --C3 monohydric and polyhydric alcohols, water-soluble C1 --C3 alkyl substituted benzene sulfonate salts, urea and mixtures thereof.
3. A detergent according to claim 1 wherein said supplementary anionic detergent is selected from the group consisting of water-soluble salts of C8 --C18 alkyl sulfates, C9 --C15 alkylbenzene sulfonates, C8 --C22 olefin sulfonates, C8 --C18 alkyl ether ethylenoxy sulfates containing an average of 1 to 4 ethylene oxide groups, C10 --C20 alkane sulfonates, C6 --C12 alkylphenyl ether ethylenoxy sulfates containing an average of 2 to 6 ethylene oxide groups, C8 --C18 alkyl sulfoacetates, N-mono-C8 --C22 alkyl sulfosuccinates, N-C8 --C18 acyl sarcosinates, N-C8 --C18 acyl taurates and O-C8 --C18 alkyl isethionates.
4. A detergent composition according to claim 3 which contains in addition from 2% to 10% by weight of an antigelling agent selected from the group consisting of sodium, ammonium or potassium formate, isethionate and mixtures thereof.
5. A detergent according to claim 4 wherein said antigelling agent is sodium formate.
6. A detergent composition according to claim 3 wherein the salt-forming cation of said alkyl ether sulfate and said supplementary anionic detergent is selected from the group consisting of sodium, potassium, ammonium and mono-, di-, or triethanolammonium.
7. A detergent composition according to claim 3 wherein said supplementary anionic detergent is a C8 --C18 alkyl sulfate or a mono-C8 --C22 alkyl sulfosuccinate.
8. A detergent composition according to claim 7 which contains in addition 2% to 10% of an antigelling agent selected from the group consisting of sodium or potassium formate, isethionate and mixtures thereof.
9. A detergent composition according to claim 8 wherein said antigelling agent is sodium formate.
10. A detergent composition according to claim 7 wherein said supplementary anionic detergent is sodium or ammonium C10 --C16 alkyl sulfate which is present in an amount of 2% to 10% by weight, said zwitterionic detergent is C8 --C18 alkanamidopropyldimethyl betaine and said alkanoic acid C2 --C3 alkanolamide is C12 --C14 alkanoic acid monoethanolamide.

This invention relates to a high-foaming liquid detergent composition which exhibits reduced detergent irritation effects when brought in contact with the skin. The inventive compositions exhibit good foaming characteristics, e.g., copious foam volume and good foam stability in the presence of grease soil, but are milder to the skin, i.e., cause less skin irritation, than currently available liquid detergents containing anionic sulfonated detergents. Thus, the inventive liquid compositions are particularly suitable for use as hand dishwashing detergents, shampoos, liquid soaps and foam baths.

Because of the known deleterious effects of the commonly used anionic detergents on the skin, research and development efforts continue unceasingly in an attempt to formulate milder liquid detergent compositions, i.e., liquid compositions exhibiting reduced skin-irritation effects.

Generally, research efforts have fallen in three categories. The first category embraces the efforts to formulate milder liquid detergent compositions by utilizing specific mixtures of particular surfactants in specific proportions. For example, U.S. Pat. No. 3,223,647 discloses mixtures of C9 --C15 alkylbenzene sulfonate and tertiary amine oxide in 20:1 to 1:5 proportions which exhibit reduced skin irritation effects. Further, U.S. Pat. No. 3,793,233 discloses mild liquid compositions containing specific proportions of an alkyl ether sulfate containing 5-12 ethylene oxide groups in the molecule, a lauryl sulfate detergent, an alkyl glyceryl ether sulfonate detergent and a trialkyl amine oxide. Similarly, U.S. Pat. No. 3,943,234 discloses a mild liquid surfactant containing trialkyl amine oxide in combination with an anionic sulfate detergent. The foregoing compositions are described as mild because the trialkyl amine oxide reduces the skin irritating effects of the lauryl sulfate and C9 --C15 alkyl benzene sulfonate detergents. However, such compositions are not completely satisfactory and the essential amine oxide surfactants may form nitrosamines which may be carcinogens.

The second category of research embraces the attempts to reduce the skin irritating effects of water-soluble anionic detergents containing sulfate, sulfonate and carboxylate solubilizing groups by addition of a specific compound. For example, U.S. Pat. No. 3,548,056 describes the addition of a protein hydrolysate having a gel strength of 0 Bloom grams to dishwashing liquids containing C9 --C15 alkylbenzene sulfonate to reduce skin irritation. Similarly, U.S. Pat. No. 4,087,518, British Pat. No. 1,122,076 and U.S. Pat. No. 4,115,548 describe the use of other protein hydrolysates or derivatives thereof to reduce the skin irritation effects of anionic sulfonate and sulfate detergents. Additionally, U.S. Pat. No. 3,944,663 discloses addition of polyethylene oxide to liquid detergents containing a mixture of C9 --C15 alkylbenzene sulfonate and C12 --C15 alkyl ether triethylenoxy sulfate to reduce the skin irritation characteristics of the liquids. However, these approaches have achieved limited success and tend to be expensive because of the high cost of the added component.

The third category of research concerns the substitution of alternative surfactants, e.g., ampholytic surfactants, nonionic surfactants, etc., for the high foaming anionic sulfate, sulfonate and carboxylate detergents. However, this approach, too, has not been successful because the ultimate products either are too costly or exhibit reduced foaming characteristics.

The present invention represents another improvement in the first category because it relates to liquid compositions which exhibit enhanced mildness, i.e., reduced skin irritation effects, without reduced foam volume and/or foam stability and/or grease emulsification properties and are based upon use of controlled proportions of specific surfactants.

As indicated above, the present invention primarily resides in the discovery that high foaming liquid detergent compositions which exhibit enhanced mildness, i.e., reduced skin irritation effects, can be achieved without any substantial sacrifice in foaming properties, e.g, foam volume and foam stability in the presence of soil, if selected proportions of four surfactants are employed. To the extent that the resultant compositions do not contain trialkyl amine oxides and do include skin-irritating sulfate, sulfonate and carboxylate detergents as one of the essential components, the achievement of liquids of improved mildness is surprising.

Broadly the present invention relates to a high foaming, liquid detergent composition having reduced skin-irritation properties which consist essentially of, by weight, 8% to 30% of an alkyl ether sulfate having the structural formula R(OC2 H4)n OSO3 M wherein R is an alkyl of 10 to 16 carbon atoms, n has an average value of 5 to 12 and M is a cation; a supplementary, water-soluble, non-soap, anionic detergent having in its molecular structure a C7 --C22 alkyl, alkenyl or acyl group and a sulfonate, sulfate or carboxylate group, the weight ratio of said alkyl ether sulfate to said supplementary detergent being in the range of 1:1 to 20:1; 1% to 8% of a zwitterionic detergent having the structural formula ##STR2## wherein R is a C8 --C18 alkyl or C8 --C18 alkanamido C2 --C3 alkyl group, R1 is C1 --C3 alkyl, R2 is a C1 --C4 alkylene or hydroxyalkylene and X is S:O or C; 1% to 8% of an N-C8 --C18 alkanoic acid C2 --C3 alkanolamide, the weight ratio of alkanolamide to said zwitterionic detergent being in the range of 1:4 to 4:1; and the balance being an aqueous medium comprising water and from 2% to 20% of a solubilizer selected from the group consisting of C2 --C3 monohydric and polyhydric alcohols, water-soluble C1 --C3 alkyl substituted benzene sulfonate salts, urea and mixtures thereof.

In a preferred aspect, the foregoing composition contains, in addition, 2% to 10% by weight of an anti-gelling agent selected from the group consisting of water-soluble salts, e.g., sodium, potassium, ammonium, etc., of formate and isethionate. More specifically, the inclusion of the anti-gelling agent results in compositions having reduced tendencies to form surface films and gels upon exposure to the atmosphere for up to twenty-four hours as compared with current present-day, commercially mild, dishwashing liquids.

The principal detergent component in the inventive liquid compositions is the water-soluble salt of a sulfuric acid ester of the reaction product of one mole of a C10 --C16 alkanol with 5 to 12 moles of ethylene oxide. These detergents are described in the prior art as alkyl ether sulfates of the following structural formula:

R(OC2 H4)n OSO3 M

wherein R is an alkyl containing about 10 to about 16 carbon atoms, n has an average value of 5 to 12 and M is a cation. Usually, the cation will be selected from the group consisting of sodium, potassium, ammonium and mono-, di- and triethanolammonium.

The methods of making the alkyl ether sulfate detergent are well known and described in issued patents. For example, the alkyl ether sulfates can be prepared by sulfating and neutralizing the reaction product of 5 to 12 moles of ethylene oxide with one mole of a C10 --C16 alkanol. Condensation of ethylene oxide and an alkanol usually is carried out under pressure in the presence of an acidic catalyst, e.g., boron trifluoride, or alkaline catalyst, e.g., sodium hydroxide. Such reaction yields a mixture of alkyl ethoxylates of varying ethylene oxide content, i.e., from one or two ethylene oxide groups per mole of alkanol to a number of ethylene oxide groups per mole of alkanol which is equal to about twice the number of moles of ethylene oxide reacted with the alkanol, with the predominant alkyl ethoxylate containing the number of moles of ethylene oxide originally reacted with the C10 --C16 alkanol. Thus, n in the formula designates the number of moles of ethylene oxide reacted with the alkanol. Sulfation of the resultant alkanol ethoxylates is achieved in a known manner using sulfur trioxide or chlorosulfonic acid as the sulfating agent. Similarly, neutralization of the sulfated product is carried out in a known manner using an aqueous base such as sodium hydroxide, ammonium hydroxide, etc.

The alkyl ether sulfate component exhibits cleaning and foaming properties and desirable mildness properties. Preferably, the alkyl ether sulfates will contain 12 to 14 carbon atoms in the alkyl group and will be employed in the form of the sodium or ammonium salt. Examples of suitable alkyl ether sulfates are sodium C12 --C14 alkyl ethylenoxy (6.5) sulfate, ammonium C12 --C14 alkyl ether ethylenoxy (6.5) sulfate, sodium C12 --C14 alkyl ether ethylenoxy (9.5) sulfate, sodium C12 --C14 alkyl ether ethylenoxy (11.4) sulfate, potassium C12 --C16 alkyl ether ethylenoxy (6.5) sulfate, ammonium C12 --C13 alkyl ether ethylenoxy (6.5) sulfate and ammonium C12 --C16 alkyl ether ethylenoxy (7) sulfate. Preferred alkyl ether sulfates are the sodium and ammonium C12 --C13 or C12 --C14 alkyl ether ethylenoxy (6.5-9) sulfates.

Generally, the mild liquid detergent compositions will contain from about 8% to 30%, preferably 12% to 24%, by weight of the alkyl ether sulfate detergent.

In addition to the primary alkyl ether sulfate detergent, the liquid composition also will include about 1% to 12%, preferably 2% to 10%, by weight of a water-soluble, supplementary, anionic detergent for the purpose of improving the detergency and foaming properties of the primary detergent. Generally, the supplementary detergent improves both the foam stability and foam volume of the primary detergent. However, the supplementary detergent has the disadvantage of being more irritating than the primary detergent which is characterized by its mildness. Thus, the concentration of the supplementary detergent is related to the concentration of the primary detergent, and the weight ratios of primary detergent to supplementary detergent usually range from about 1:1 to about 20:1, preferably 1.5:1 to 6:1.

Satisfactory supplementary detergents are water-soluble, non-soap, anionic detergents having in their molecular structure a C7 --C22 alkyl, alkenyl or acyl group and a sulfonate, sulfate or carboxylate group. Such detergents are employed in the form of water-soluble salts and the salt-forming cation usually is selected from the group consisting of sodium, potassium, ammonium, and mono-, di- or tri-C2 --C3 alkanolammonium, with the sodium and ammonium cations again being preferred.

The suitable supplementary anionic detergents include the following:

1. The C8 --C18 alkyl sulfates which are usually obtained by sulfating C8 --C18 alkanols obtained by reducing the glycerides of tallow or coconut oil. Preferred alkyl sulfates contain 10 to 16 carbons in the alkyl group.

2. The C9 --C15 alkylbenzene sulfonates wherein the alkyl group is either a straight chain or a branched chain, with the straight chain being preferred for its improved biodegradability.

3. The C8 --C22 olefin sulfonates which may be obtained by sulfating the appropriate olefin. Preferred olefin sulfonates contain from 14 to 16 carbon atoms in the alkyl group and are obtained by sulfonating an α-olefin.

4. The C8 --C18 alkyl ether ethylenoxy sulfates of the formula

R(OC2 H4)n OSO3 M

wherein n is 1 to 4. These sulfates differ from the primary alkyl ether sulfate detergent in the number of moles of ethylene oxide (1-4) reacted with one mole of alkanol in forming the ethoxylated alkanol which is sulfated and neutralized to form this anionic detergent. Preferred alkyl ether ethylenoxy sulfates contain 12 to 16 carbon atoms in the alkyl group and contain two to three ethylene oxide groups per mole of alkanol.

5. The C10 --C20 paraffin sulfonates obtained, for example, by reacting an α-olefin with bisulfite. Preferred alkane sulfonates contain 13 to 17 carbon atoms in the alkyl group.

6. The C6 -C12 phenyl ether polyethylenoxy sulfates containing from 2 to 6 moles of ethylene oxide in the molecule may be used, too. These detergents can be prepared by reacting an alkyl phenol with 2 to 6 moles of ethylene oxide and sulfating and neutralizing the resultant ethoxylated alkylphenol. Preferred detergents in this group have 8 to 12 carbons in the alkyl group and contain about 4 ethylene oxide groups in the molecule.

7. The C8 --C18 alkyl sulfoacetates corresponding the formula

ROOCCH2 SO3 M

wherein R is a C8 -C18 alkyl which may be prepared by esterifying an alkanol with chloroacetic acid or chloroacetyl chloride and then reacting the chloroester with a sodium or potassium bisulfite. Preferred sulfoacetates contain 12 to 16 carbon atoms in the alkyl group.

8. The N-mono-C8 --C22 alkyl (includes alkyl groups interrupted by an ether or amido group) sulfosuccinates prepared by reacting, for example, either one mole of C8 --C18 alkanol or a C8 --C18 alkoxy C2 --C3 alkanol or a C8 --C18 alkanamido C2 --C3 alkanol with maleic acid and reacting the resultant product with an alkali metal bisulfite to form an N-mono-C8 --C22 alkyl sulfosuccinate. It should be recognized that the alkyl group of product made from the N-acyl alkanolamine will contain an amido intermediate linkage. Similarly, the alkyl group may be interrupted by an ether linkage or ester linkage if an alkyl ether ethanol or an alkyl ester of ethylene glycol is reacted with maleic acid. Preferred sulfosuccinates are disodium N-mono-C8 --C18 acylisopropanolaminosulfosuccinate, disodium lauryl sulfosuccinate and N-monooleylisopropanolaminosulfosuccinate.

9. The N-C8 --C18 acyl sarcosines may be produced by neutralizing the reaction product of a C8 --C18 alkanoic acid with N-methyl glycine. Preferred sarcosinates contain 12 to 14 carbon atoms in an acyl group obtained by reduction of coconut oil.

10. The N-C8 --C18 acyl taurines may be produced by neutralizing the reaction product of a C8 --C18 alkanoic acid with aminoethylsulfonic acid. Again, preferred taurates contain 12 to 14 carbon atoms in an acyl group obtained by reduction of coconut oil.

11. The O-C8 --C18 acyl isethionates may be produced by neutralizing the reaction product of a C8 --C18 alkanoic acid with 2-hydroxyethanesulfonic acid. Similar to the sarcosines and taurines, the preferred isethionates contain 12 to 14 carbon atoms in an acyl group obtained by reduction of coconut oil.

As indicated above, the proportion of the supplementary anionic detergent must be controlled if the final composition is to be mild to the skin because the supplementary anionic detergents are more irritating to the skin than the principal alkyl ether sulfate detergent. For example, the patent art clearly indicates that C8 --C18 alkyl sulfates and C9 --C15 alkyl benzene sulfonates are irritating to the skin. Furthermore, the other supplementary anionic detergents suitable for use herein also are irritating to the skin, but usually to a lesser degree than the alkyl sulfate and alkylbenzene sulfonate detergents. Although the supplementary detergents are included to improve the foaming and detergency properties of the inventive liquid compositions, it should be understood that the concentration present will be maintained at the minimum level consistent with the desired performance characteristics in order to preserve the mildness of the final product. Thus, the proportions of the individual supplementary anionic detergents are variable and will be based upon an appropriate integration of foaming, cleaning and mildness properties of the individual supplementary detergents with the principal alkyl ether sulfate detergent.

The third essential ingredient in the inventive, mild, liquid compositions is a zwitterionic detergent corresponding to the formula ##STR3## wherein R is a C8 --C18 alkyl or C8 --C18 alkanolamido C2 --C3 alkyl, R1 is C1 --C3 alkyl, R2 is a C1 --C4 alkylene or C1 --C4 hydroxy alkylene and X is C or S:O. When X is C, the detergent is called a betaine, and when X is S:O, the detergent is called a sultaine or sulfobetaine. These zwitterionic detergents can be described broadly as derivatives of aliphatic quaternary ammonium or tertiary sulfonium compounds containing a C8 --C18 aliphatic radical which may be straight chained or branch chained and containing an anionic group. Preferred betaine and sultaine detergents are lauryldimethylammonioacetate, myristyldimetylammonioacetate, C8 --C18 alkanamidopropyldimethylammonio acetate 1-(myristyldimethylammonio)-propane-3-sulfonate and 1-(myristyldimethylammonio)-2-hydroxypropane-3-sulfonate.

In the inventive compositions, the zwitterionic detergent acts as both a foam builder and as a counter-irritant detergent. Generally, the proportion of zwitterionic detergent in the liquid compositions will range from 1% to 8%, preferably 2% to 6%, by weight. Further, the proportion of zwitterionic detergent will be integrated with the proportion of the supplementary anionic detergent in view of its apparent counter irritant effects and, desirably, the weight ratio of zwitterionic to supplementary anionic will be from 2:1 to 1:3. Additionally, the zwitterionic detergent concentration will be coordinated with the alkanoic acid alkanolamide foam booster in order to achieve liquid compositions of optimum foam stability.

The final essential ingredient in the mild liquid detergent compositions will be a C8 --C18 alkanoic acid C2 --C3 alkanolamide. This component is widely recognized as a foam builder and satisfactory alkanoic acid alkanolamides are lauric monoethanolamide, myristic monoethanolamide, lauric diethanolamide, myristic diethanolamide, lauric isopropanolamide and coconut (C8 C18) monoethanolamide. Preferred alkanoic acid alkanolamides contain 12 to 14 carbons in the fatty acyl group. A particularly preferred compound is lauric-myristic monoethanolamide.

As stated above, the proportions of the essential alkanoic acid alkanolamide and the essential zwitterionic detergent are controlled in the range of 1:4 to 4:1, preferably from 1:2 to 2:1 in order to achieve optimum foam stability. Both the zwitterionic detergent and alkanoic acid alkanolamide must be present because the desired foam stability cannot be achieved when only one of these compounds is present. Usually, the amount of alkanoic acid alkanolamide in the liquid detergent composition will be 1% to 8%, preferably 2% to 6%, by weight.

Usually, the balance of the liquid composition will be an aqueous medium comprising water and about 2% to 20%, preferably 4% to 14%, by weight of a solubilizer selected from the group of C2 --C3 monohydric and polyhydric alcohols, water-soluble C1 --C3 alkyl substituted benzene sulfonates, urea and mixtures thereof. Suitable monohydric alcohols are ethanol and isopropanol, with ethanol being preferred. Suitable C1 --C3 alkylbenzene sulfonates are sodium, potassium and ammonium salts such as sodium xylene sulfonate, potassium toluene sulfonate and sodium isopropylbenzene sulfonate. Typically, the solubilizer is selected to provide clarity and/or low-temperature cloud point and/or to control viscosity. Since the alcohol and sulfonate solubilizers do not exhibit the same effects, usually the liquid compositions herein will contain a mixture of alcohol and hydrotropic sulfonate. Also, urea may be included as a solubilizer where the desired low-temperature cloud temperature or viscosity cannot be achieved in its absence.

In the preferred liquid compositions, from 2% to 10%, preferably, 4% to 8%, by weight of an anti-gelling agent selected from the group consisting of sodium, ammonium or potassium formate and sodium, ammonium or potassium isethionate will be present. Such agent inhibits the tendency of the liquid compositions to form surface films and gels when the composition is in contact with the atmosphere for up to twenty-four hours--a condition which might occur if the cap inadvertently is left off of a container of a product after use. Gelling is determined by pouring 30 millileters (ml) of product into a 50 ml. beaker and observing the surface and contents after 1/4, 1/2, 1, 2, 3, 4, 5, 6, 7 and 24 hours. The product is rated for film and/or gel formation on a scale of 0 to 10 at each observation. The gel value is the sum of the ratings. Compositions containing the anti-gelling agent exhibit superior anti-gelling tendencies as compared with a leading mild liquid detergent.

The described mild liquid compositions are essentially unbuilt liquids, i.e., do not contain proportions of organic or inorganic builder salt in detergent building proportions, and, therefore, are suitable for use as liquid, hand dishwashing detergents, liquid shampoos, liquid hand soaps and foam or liquid shower bath products. Thus, these inventive compositions can contain any of the usual adjuvants found in those compositions provided that they do not interfere with the mildness or performance properties of the imventive liquids. Such additional ingredients include minor proportions of perfumes and colors for aesthetic purposes, opacifiers such as ethylene glycol distearate or polystyrene, thickening agents such as gums or hydroxypropyl methyl cellulose, sequestering agents such as citrate or ethylenediamine tetraacetate, preservatives such as formaldehye or Dowicil®200 or monomethyloldimethyl hydantoin, fluorescent agents or optical whiteners, magnesium sulfate and inert salts such as sodium sulfate. The total concentration of added ingredients usually will be less than 5%, preferably less than 3%, by weight of the total composition.

These compositions are prepared by admixing the individual detergent ingredients with the formula weight of water with agitation at a temperature in the range of about 32°C to 65°C Usually the individual detergents are added in the form of aqueous solutions or dispersions. Typically, the alkanoic acid alkanolamide is added in liquid form as one of the last ingredients at a temperature below about 55°C Also, when present, the anti-gelling agent is added to the formula weight of water as the first ingredient or to a surfactant-water mixture in order to dissolve it. Additionally, it is desirable to add any solubilizing agent to the formula weight of water prior to the addition of the essential detergent ingredients in order to avoid formation of gels. Any additional ingredients, such as color and perfume usually are added with agitation after the alkanolamide while cooling the mixture to 25°C to 32°C temperature. The pH is usually adjusted, if necessary, to a pH in the range of 5-9, preferably 6.5-8.5, for dishwashing and shampoo products by addition of, for example, either sulfuric acid or citric acid or sodium hydroxide, potassium hydroxide or triethanolamine. Further, any adjustment of viscosity may be achieved by adding additional amounts of the appropriate solubilizers or thickening agents.

Usually, the viscosity of the liquid compositions will be variable over the range of about 20 centipoises (cps) to 2000 cps., and preferably from 75 cps. to 1000 cps. Viscosity is measured using a Brookfield Viscometer, Model LVF, with a #1 spindle rotating at 12 r.p.m. The most preferred viscosity range is 150 cps. to 350 cps. based upon current consumer preferences. However, it will be recognized by one skilled in the art that liquids of even higher viscosity can be achieved by including up to 2% by weight of a known thickening agent in the inventive compositions.

The foaming and grease emulsification characteristics of the inventive liquid compositions are illustrated in the following dishwashing test. In this test, ceramic dinner plates having a diameter of nine and one-half inches soiled with about 4 grams of Crisco® or about 15 grams of Ragu® spaghetti sauce soil are washed at thirty second intervals in a dishpan containing either six grams (0.1%) or 12 grams (0.2%) of liquid composition dissolved in six liters of water of a selected hardness at a temperature of about 46°C (Six grams of detergent are employed when each plate is soiled with Ragu® spaghetti sauce and twelve grams are employed when each plate is soiled with Crisco at the beginning of the test.) A layer of foam is generated by allowing the six liters of water to fall from a separatory funnel mounted sixteen inches above the bottom of the dishpan into a Petri dish containing the liquid composition to be tested which is located in the center of the dish pan. The Petri dish is removed carefully and the foam height is measured prior to the start of the test. A soiled dish is placed in the solution every thirty seconds and is washed by the operator for 10 to 15 seconds while holding it about half in and half out of the solution. Washing continues until about one half of the surface of the dish pan is covered with foam. Usually, a control is run at the same time as the test product in order to eliminate any differences due to different operators. Results are reproducible and a difference of 2 plates is considered to be significant.

Specific inventive liquid compositions are illustrated by the following examples. All quantities indicated in the examples or elsewhere in the specification are by weight unless otherwise indicated.

A preferred dishwashing liquid composition according to this invention follows:

______________________________________
% by weight
______________________________________
Sodium C12 -C14 alkyl ether ethylenoxy
16
(6.5) sulfate(a)
Ammonium lauryl sulfate
6
Cocoamidopropyldimethylbetaine
4
Lauric-myristic monoethanolamide
3
Ethanol 4
Sodium xylene sulfonate
1.8
Sodium formate 6.0
Hydroxyethyl ethylene diamine
0.2
tri-acetic acid, tri-sodium salt (HEDTA)
Water, color, perfume balance
100.0
______________________________________
(a) Weight ratio of C12 to C14 is 82% to 18%

This composition is prepared by dissolving the sodium formate in water and thereafter adding the sodium alkyl ether ethylenoxy sulfate, the betaine and the ammonium lauryl sulfate while agitating moderately. The sodium alkyl ether ethylenoxy sulfate is added as an aqueous alcoholic solution containing 52.3% by weight of said sulfate and 13% by weight of ethanol. Additionally, both the betaine and the ammonium lauryl sulfate are added as aqueous solutions containing 30% by weight of said ingredient. Thereafter, a mixture of lauric-myristic monoethanolamide, sodium xylene sulfonate and water (40% by weight of amide, 24% by weight of sodium xylene sulfonate and 36% by weight of water) is added at a temperature of 40°C to 47°C in the presence of moderate agitation. Finally, perfume, color and sesquestrant are added with agitation and the pH is reduced from 8.1 to 7.35 with concentrated sulfuric acid.

The resultant product is a clear liquid at 25°C having a specific gravity of 1.07 and a viscosity of 405 centipoises (cps) as measured with a Brookfield Viscometer, Model LVF, rotating at 12 rpm using a #1 spindle. Such product exhibits a cloud point of about 5°C and is free of gelling tendencies upon exposure to the atmosphere for a period of twenty-four hours.

Examples 2A-2D which follow illustrate the effect of increased ethanol concentrations in the composition of Example 1 on the viscosity and cloud point of the resultant product. In these compositions, the additional ethanol replaced a light weight of water.

______________________________________
Example 2A 2B 2C 2D
______________________________________
% ethanol 4.5 5.0 5.5 6.0
Viscosity 300 255 200 165
(cps)
Cloud 1 0 0 0
point (°C.)
______________________________________

All of the foregoing compositions exhibited no gelling tendencies when left exposed to the atmosphere for up to twenty-four hours.

Other satisfactory single-phase liquid dishwashing compositions are described below:

__________________________________________________________________________
Example
Ingredient 3 4 5 6 7 8 9 10
__________________________________________________________________________
Alkyl ether ethylenoxy
16(a)
16(a)
16(a)
16(a)
16(a)
16(b)
16(b)
16(b)
(6.5) sulfate salt
Ammonium lauryl sulfate
6
Sodium linear dodecylbenzene
6
sulfonate
Sodium C12 -C15 alkyl ether
6
ethylenoxy (3) sulfate
Sodium C14 -C16 alpha olefin
6
sulfonate
Sodium lauryl sulfoacetate 6
Disodium lauroylamidoisopropyl 8
sulfosuccinate
Sodium lauroyl isethionate 8
Sodium C8 -C18 acyl N--methyl taurate
8
Cocoamidopropyldimethyl betaine
4 4 4 4 4 4 4 4
Lauric myristic monoethanolamide
3 3 3 3 3 4 4 4
Sodium xylene sulfonate
5.4
5.4
5.4
5.4
5.4
5.4
6.5
6.5
Ethanol 8.1
8.1
9.5
8.1
8.1
9.6
9.6
9.6
Water, perfume, color
balance
__________________________________________________________________________
(a)Ammonium salt of C12 -C13 (41%/57%) alkyl ethylenoxy ether
sulfate
(b)Ammonium salt of C12 -C14 (55%/45%) alkyl ethylenoxy ether
sulfate

The cleaning and foaming characteristics of the compositions Examples 1 and 3-10 are compared with two leading brands of dishwashing detergents, one of which is a leading mild dishwashing liquid, in the hand dishwashing evaluation test described herein. The performance results are set forth in Table I below:

TABLE I
______________________________________
Number of Plates washed
Ragu Spaghetti
Composition Crisco Soil
Sauce Soil
______________________________________
Example 1 18 30
Example 3 19 34
Example 4 16 31
Example 5 16 30
Example 6 17 35
Example 7 16 29
Example 8 16 33
Example 9 17 35
Example 10 18 33
Leading Brand A
16 33
Leading Brand B
19 29
______________________________________

As shown by the results in the foregoing table, the compositions of the invention are characterized by cleaning and foaming properties which are equal to or superior to comparable commercial dishwashing liquids. Such results are particularly significant because the amounts of detergent active materials in leading Brands A and B are 34% and 33.5% respectively as compared with 29% for the compositions of Examples 1 and 3-7 and 32% for the compositions of Examples 8-10. Thus, the inventive composition exhibit an advantage based upon the performance obtained per part of detergent active material.

In order to evaluate the mildness properties of the compositions of this invention, two different tests are used. One test is an in vivo skin irritation test using quinea pigs. The second test is an in vivo skin irritation test on human subjects.

In the guinea pig test, the abdomen is shaved one day prior to the initiation of the test, an appropriate concentration of the product in water selected from the range of about 0.5% to 20% is selected for testing and one c.c. of the test solution is applied to the two separate areas about one square inch on the shaved abdomen of the test animal. Said area is covered with a patch which is removed after four hours. The foregoing procedure is repeated on the second and third days using different sites on the animal's abdomen. On the sixth day, any hair which has grown is removed with a commercial hair removing product and the test animal is thoroughly rinsed with water and dried. Four hours later each of the test sites is rated by a skilled observer for irritation, i.e., scaling, redness, cracking and visible sores, on a scale of 0-4. A rating of 0 corresponds to no irritation and a rating of 4 indicates visible sores and cracking. The ultimate irritation valve represents the average of six ratings. A difference in rating of 0.7- 1 is considered to be significant.

In the in vivo test on human subjects, a panel of from 25 to 30 subjects is employed. Again, 0.2 ml. of a solution of the desired product concentration is applied to an area of approximately one square inch on the back of each subject and such area is covered with a patch. After 231/2 hours the patch is removed and one-half hour later the degree of irritation at the test site is rated by a dermatologist using the 0 to 4 scale employed in the in vivo quinea pig test above. The test protocol is repeated fifteen more times, with the test solution being applied to the same test area each time. On weekends, the patch is not removed and the irritation is rated seventy-two hours after the preceeding application. Thus, sixteen readings are obtained over the course of a twenty-one day period. At the conclusion of the test, the cumulative score for each individual is determined and the irritation value for each product is equal to the sum of the scores of all of the members of the panel. Each panelist may wear up to 8 or 9 patches on his back and, therefore, up to nine products may be evaluated in a single test. The detailed test method is described in the article by Phillips et al. at pages 369-382 of the Journal of Toxicology and applied Pharmacology, 21 (1972).

Table 2 below shows some of the results from the in vivo quinea pig test.

TABLE 2
______________________________________
Irritation Scores in In Vivo Guinea Pig Test
Irritation Score
Composition 2% Solution(a)
3% Solution(a)
______________________________________
Example 3 1.5 1.4
Example 4 0.9 1.0
Example 6 1.2 1.5
Leading Brand B
2.2 3.0
______________________________________
(a) Concentration of the product in water

The test results clearly show that the inventive compositions are milder than Leading Brand B which is a leading mild liquid detergent.

The mildness of the inventive compositions is confirmed by the results obtained using a panel of twenty-five persons in the in vivo human subject test described above. In this test three concentrations of each of three products were determined and the results are shown in Table 3 below.

TABLE 3
______________________________________
Irritation Scores in In Vivo Human Test
Irritation Score
1% 5% 10%
Composition Solution(a)
Solution(a)
Solution(a)
______________________________________
Example 1 31 25.5 38
Example 3 55 74 73
Leading Brand B
50 73 135.5
______________________________________
(a) Concentration of the product in water

Based upon the foregoing results, the inventive compositions are as mild or milder than a leading mild brand, particularly at high concentrations. Such results substantially correspond to the results obtained in the in vivo guinea pig test and confirm the validity and utility of that test.

Two statistical analyses of the data summarized in Table 3 showed leading brand B to be significantly more irritating than either inventive product at the 10% concentration. Furthermore, a second statistical analysis of the data after deletion of the scores of a single subject who appeared to be a statistical outlier indicated leading brand B to be significantly more irritating than Example 1 at 1% and 5% concentrations. This second statistical analysis again indicated no statistical difference between the compositions of Examples 1 and 3.

The following compositions show the effect of increasing amounts of sodium xylene sulfonate solubilizer on the appearance and gelling tendencies of the inventive compositions:

__________________________________________________________________________
11 12 13 14 15 16
__________________________________________________________________________
Sodium C12 -C14 alkyl ether
16 16 16 16 16 16
ethylenoxy sulfate(a)
Ammonium lauryl sulfate
6 6 6 6 6 6
Cocoamidopropyl dimethyl
betaine
Lauric-myristic
3 3 3 3 3 3
monoethanolamide
Ethanol 4 4 4 4 4 4
Sodium xylene sulfonate
2.8 3.8 4.8 5.8 6.8 7.8
Water, color, perfume
balance
100 100 100 100 100 100
Appearance at 24°C
Hazy
Clear
Clear
Clear
Clear
Clear
Gelling value -- 74 57 33 0 0
Cloud point (°C.)
-- -- -- -- -- 4°C
__________________________________________________________________________
(a) Weight ratio of C12 to C14 is 55% to 45%.

These compositions show that a solubilizer is necessary to achieve clarity at room temperature (25°C) and that gelling tendencies decrease as the concentration of sodium xylene sulfonate increases from 2.8% to 7.8% in combination with 4% of ethanol.

The composition of Example 1 is repeated with the exception that the concentration of sodium formate is changed from 6% to 4%, 8% and 10% respectively, with the concentration of water being adjusted accordingly. The resultant compositions are clear liquids at 25°C and the effect of the concentration of sodium formate on the gelling value is set forth in Table 4.

TABLE 4
______________________________________
% Sodium Formate
Gelling Value
______________________________________
4% 48
8% 2
10% 3
______________________________________

As the gelling value of the composition which does not contain any sodium formate is 76, it is clear that 4% or more of sodium formate is effective to reduce the gelling tendency.

Other suitable compositions follow together with pertinent physical property information.

______________________________________
% by weight
21 22
______________________________________
Ammonium C12 -C13 alkyl ethylenoxy
16 16
(6.5) sulfate(a)
Ammonium lauryl sulfate
6 6
Cocoamidopropyldimethyl betaine
4 4
Lauric-myristic monoethanolamide
3 3
Ethanol 3.1 3.1
Sodium xylene sulfonate
3.8 3.8
HEDTA 0.2 0.2
Sodium formate 5.0 3.0
Water, perfume, color balance
100.0 100.0
Appearance at 25°C
Clear Clear
Viscosity at 25°C (cps.)
340 26
Specific gravity 1.067 1.056
Gelling value 0 29
______________________________________
(a) Weight ratio of C12 to C13 is 41% to 57%

The following compositions containing lauric-myristic diethanolamide were clear liquids at 25°C, but exhibited gelling tendencies.

______________________________________
% by weight
23 24 25
______________________________________
Sodium C12 -C14 alkyl ether ethylenoxy
16 16 16
(6.5) sulfate(a)
Sodium alpha C14 -C16 alkenyl sulonate
6 6 6
Cocoamidopropyldimethylbetaine
4 4 4
Lauric myristic diethanolamide
4 5 6
Sodium xylene sulfonate
3.8 3.8 3.8
Ethanol 4.7 4.7 4.7
Hydroxyethyl ethylene diamine,
0.2 0.2 0.2
triacetic acid, trisodium salt
Water, color, perfume
balance
100 100 100
Viscosity at 25°C (cps.)
65 135 235
______________________________________
(a) Weight ratio of C12 /C14 is 45% to 55%
______________________________________
% by weight
26 27
______________________________________
Ammonium C12 -C13 alkyl ether ethylenoxy
16 16
(6.5) sulfate(a)
Disodium cocoamidoisopropyl sulfosuccinate
8 8
Cocoamidopropyldimethylbetaine
4 4
Lauric-myristic monoethanolamide
4 4
Sodium formate -- 1.5
Ethanol 3.1 3.1
Sodium xylene sulfonate 2.4 2.4
Water, perfume, color balance
100.0 100.0
Appearance at 25°C
Clear Clear
Viscosity at 25°C
140 175
Specific gravity 1.052 1.070
Gelling value 5 4
______________________________________
(a) Weight ratio of C12 to C13 is 41% to 57%

In the hand dishwashing test, the composition with the same detergent actives as Example 26 washed 18 plates soiled with Crisco® and 33 plates soiled with Ragu® spaghetti sauce. These compositions also are effective when used to shampoo the hair or to wash the hands.

When either disodium oleylamidoisopropyl sulfosuccinate or disodium lauryl sulfosuccinate is substituted for the disodium cocoamidoisopropyl sulfosuccinate in the composition of Example 26, substantially identical dishwashing results are obtained.

Other suitable liquid compositions follow together with detergency results:

______________________________________
% by weight
28 29 30
______________________________________
Sodium C12 -C14 alkyl ether
16 19
ethylenoxy (11.4) sulfate
Sodium C12 -C14 alkyl ether
16
ethylenoxy (6.5) sulfate
Ammonium lauryl sulfate
6 -- --
Sodium dodecylbenzene
-- 4 --
sulfonate
Sodium lauroyl sarcosinate
-- -- 6
dimethyl
Cocoamidopropyl/betaine
4 3 4
Lauric-myristic mono-
3 4 3
ethanolamide
Ethanol 8.7 9.4 8.1
Sodium xylene sulfonate
5.4 6.2 5.4
Water, perfume, color
balance
100 100 100
Plates washed (Crisco)(R)
16 14 15
Plates washed (Ragu(R) sauce)
33 28 31
______________________________________

Compositions containing other zwitterionic detergents follow together with plate washing results:

______________________________________
% by weight
31 32 33
______________________________________
Ammonium C12 -C13 alkyl ether
16 16 16
ethylenoxy (6.5) sulfate(a)
Ammonium lauryl sulfate
6 6 6
3-Cocamidopropyl dimethyl sulfobetaine
4
C8 -C18 alkyl dimethyl betaine
4
Lauryldimethyl betaine 4
Lauric-myristic mono-ethanolamide
3 3 3
Ethanol 8.1 8.1 8.1
Sodium xylene sulfonate
5.4 5.4 5.4
Water, perfume, color balance
100 100 100
Plates washed (Crisco(R))
16 18 18
______________________________________
(a) Weight ratio of C12 to C13 is 41% to 47%

Other compositions suitable for use as foam baths, shampoos or dishwashing detergents follow:

______________________________________
% by weight
35 36 37 38
______________________________________
Ammonium C12 -C14 alkyl ether
13 19 19 22
ethylenoxy sulfate (6.5 EO)
Ammonium laurylsulfate
2 6 2 4
Cocoamidopropyldimethyl betaine
4.5 1.5 4.5 3
Lauric-myristic monoethanolamide
1.5 4.5 4.5 3
Ethanol 9.2 11.2 11.2 12.1
Sodium xylene sulfonate
4.2 6.6 6.6 5.4
Water, perfume, color
balance
100 100 100 100
Planchets washed (Crisco(R))(b)
14 20 16 18
______________________________________
(a) Weight ratio of C12 to C14 is 82% to 18%
(b) Number of planchets washed using a Tergotometer foam test wherei
aluminum planchets (1inch diameter and 1/8 inch high) each soiled with on
gram of Crisco(R) soil are added at twominute intervals to 500 mls o
solution containi ng 0.1% by weight of the test composition maintained at
50°C In this test, an initial foam volume is generated by
agitation of 250 ml of solution containing the test composition for five
minutes followed by addition of 250 ml of water and a furthe r one minute
period of agitation. Agitation ceases for one minute during which period
one planchet is added. Agitation resumes for one minute and then ceases
for one minute, with the foam volume being read and a planchet being adde
while the agitator i s stopped. This cycle is repeated until the surface
is not completely covered with foam. The number of planchets washed prior
to the end of the test is recorded. The number of planchets washed
substantially corresponds to the number of plates washed in the
handdishwashing test.

The compositions of Examples 35-38 compare favorably with the dishwashing results for leading brand A--16 planchets--and for leading brand B--21 planchets.

______________________________________
% by weight
______________________________________
Ammonium C12 -C13 alkyl
20
ether ethylenoxy (6.5) sulfate
Ammonium Lauryl sulfate
4
Cocoamidopropyldimethyl betaine
5
Lauric-myristic mono-ethanolamide
5
HEDTA 0.2
Ethanol 3.5
Sodium xylene sulfonate
5.3
Sodium formate 6
Magnesium sulfate heptahydrate
1
Water, color, perfume balance
100
Appearance at 25°C
Clear
Viscosity (cps.) 250
Specific gravity 1.075
Plates washed (Crisco(R))
20
Plates washed (Ragu(R) sauce)
36
______________________________________

The foregoing composition is higher foaming and exhibits better grease soil emulsification properties than leading brand B.

In its broadest form, the present invention relates to a high foaming detergent composition having reduced skin-irritation properties wherein the active detergent ingredient comprises a mixture of, by weight, 8 to 30 parts of an alkyl ether sulfate having the structural formula

R(OC2 H4)n OSO3 M

wherein R is an alkyl of 10 to 16 carbon atoms, n has an average value of 5 to 12 and M is a cation; a supplementary, water-soluble, non-soap, anionic detergent having in its molecular structure a C7 --C22 alkyl, alkenyl or acyl group and a sulfonate, sulfate or carboxylate group, the weight ratio of said alkyl ether sulfate to said supplementary degergent being in the range of 1:1 to 20:1, 1 to 8 parts of a zwitterionic detergent having the structural formula ##STR4## wherein R is a C8 --C18 alkyl or C8 --C18 alkanamido C2 --C3 alkyl group, R1 is a C1 --C3 alkyl group, R2 is a C1 --C4 alkylene or hydroxyalkylene group and X is S:O or C, and 1 to 8 parts of an N-C8 --C18 alkanoic acid C2 --C3 alkanolamide, the weightratio of said alkanolamide to said zwitterionic detergent being in the range of 1:4 to 4:1. Such active ingredient mixture may be used in admixture with other ingredients normally found in high foaming detergent compositions, particularly those detergent compositions whose aqueous solutions come in contact with the skin or hair of the user.

The invention has been described with respect to various examples and illustrations thereof but is not to be limited to these because it is clear that one of skill in the art, with the present description before him, will be able to utilize substitutes and equivalents without departing from the invention.

Robbins, Clarence R., Lai, Kuo-Yann, Klisch, Stephen C.

Patent Priority Assignee Title
4671894, Nov 07 1984 PROCTER AND GAMBLE COMPANY, THE, CINCINNAT, OH , A CORP OF OH Liquid detergent compositions
4692275, Apr 23 1986 Lever Brothers Company Detergent compositions containing an alkylbenzene sulfonate and alcohol ethoxysulfate surfactant system
4731201, Aug 12 1986 Colgate-Palmolive Company; COLGATE-PALMOLIVE COMPANY, 300 PARK AVENUE, NEW YORK, NEW YORK 10022, A CORP OF DE Shampoo method and composition
4732707, Aug 17 1984 Lever Brothers Company Detergent compositions containing special alkyl ether sulphate in combination with alkylbenzene sulphonate and/or dialkyl sulphosuccinate esters
4772424, Jan 08 1986 The Proctor & Gamble Company; Procter & Gamble Company, The Shampoo containing mixtures of sulfate and/or sulfonate, sarcosinate and betaine surfactants
4772425, Dec 23 1985 COLGATE-PALMOLIVE COMPANY, A CORP OF DE Light duty liquid dishwashing composition containing abrasive
4851154, Apr 10 1987 L'Oreal Detergent and foaming cosmetic composition delaying the regreasing of hair
4917842, Feb 12 1988 The Standard Oil Company Process of making ceramics
4931204, Nov 14 1988 PEOPLE S BANK Self-foaming oil compositions and process for making and using same
4979993, Mar 27 1989 Loctite Corporation Trialkylammonium alkyl carboxylate primer for cyanoacrylate bonding of polymeric substrates
4992213, Jun 23 1989 Cleaning composition, oil dispersant and use thereof
5057246, Jul 25 1986 HENKEL ENTRETIEN A COMPANY OF FRANCE Viscous detergent composition capable of being diluted and process for producing it
5066743, Mar 27 1989 Loctite Corporation Two-part composition comprising a cyanoacrylate adhesive and a primer comprising a tertiary ammonium carboxylate compound
5075042, May 01 1989 MORRISON, JOYCE L Surfactant blend containing an alkyl poly(ethyleneoxy)sulfonate to reduce dermal irritation
5167872, Oct 31 1985 The Procter & Gamble Company Comprising anionic surfactant polymeric nonionic surfactant and betaine surfactant
5186857, Nov 14 1988 PEOPLE S BANK Self-foaming oil compositions and process for making and using same
5298195, Mar 09 1992 Access Business Group International LLC Liquid dishwashing detergent
5310508, Jul 15 1992 Colgate-Palmolive Company Mild personal cleansing compositions containing sodium alcohol ethoxy glyceryl sulfonate
5336445, Mar 27 1990 The Procter & Gamble Company Liquid hard surface detergent compositions containing beta-aminoalkanols
5336446, Feb 21 1989 Compositions and process for non-irritating dense foaming of bath water and peri-vaginal cleaning
5342549, Jan 29 1990 The Procter & Gamble Company Hard surface liquid detergent compositions containing hydrocarbyl-amidoalkylenebetaine
5415810, Nov 05 1991 Lever Brothers Company, Division of Conopco, Inc. Detergent composition
5443757, Mar 09 1992 Access Business Group International LLC Liquid dishwashing detergent
5454983, Jan 23 1992 The Procter & Gamble Company Liquid hard surface detergent compositions containing zwitterionic and cationic detergent surfactants and monoethanolamine and/or beta-aminoalkanol
5512212, Feb 25 1994 Betz Laboratories, Inc. Corrosion inhibitor composition and method of use
5531933, Dec 30 1993 The Procter & Gamble Company; Procter & Gamble Company, The Liquid hard surface detergent compositions containing specific polycarboxylate detergent builders
5534198, Aug 02 1994 The Procter & Gamble Company; Procter & Gamble Company, The Glass cleaner compositions having good filming/streaking characteristics and substantive modifier to provide long lasting hydrophilicity
5536450, Nov 12 1993 The Procter & Gamble Comany Liquid hard surface detergent compositions containing amphoteric detergent surfactant and perfume
5536451, Oct 26 1992 Procter & Gamble Company, The Liquid hard surface detergent compositions containing short chain amphocarboxylate detergent surfactant
5540864, Dec 21 1990 The Procter & Gamble Company Liquid hard surfce detergent compositions containing zwitterionic detergent surfactant and monoethanolamine and/or beta-aminoalkanol
5540865, Jan 29 1990 The Procter & Gamble Company Hard surface liquid detergent compositions containing hydrocarbylamidoalkylenebetaine
5565421, Nov 16 1993 Colgate Palmolive Co. Gelled light duty liquid detergent containing anionic surfactants and hydroxypropyl methyl cellulose polymer
5602087, Aug 02 1994 Colgate-Palmolive Company; Colgate - Palmolive Company Composition
5683972, Dec 20 1993 Colgate-Palmolive Company Foaming oil-in-water emulsion
5686400, Aug 05 1994 Cognis Corporation Manual dishwashing method using betaine-anionic surfactant mixtures
5726137, Jun 21 1989 Colgate-Palmolive Company Low silicone hair conditioning shampoo and non-silicone hair conditioning/style control shampoo
5888960, Jun 01 1995 Cognis Corporation Surfactant composition
5929024, Nov 20 1997 Colgate Palmolive Company Cleaning compositions
6524390, May 16 1995 Handwashing technique analysis
8801955, Sep 03 2004 Industry-Academic Cooperation Foundation, Yonsei University Water-soluble nanoparticles stabilized with multi-functional group ligands and method of preparation thereof
Patent Priority Assignee Title
3755206,
3793233,
3898186,
3944663, Jun 16 1971 Colgate Palmolive Company Mild light duty detergent containing homopolymers of ethylene oxide
3950417, Feb 28 1975 Johnson & Johnson High-lathering non-irritating detergent compositions
4092273, Oct 03 1974 Colgate-Palmolive Company Liquid detergent of controlled viscosity
4221733, Nov 12 1977 REWO CHEMISCHE WRKE GMBH, STEINAU AN DER STRASSE, GERMANY Betaines exhibiting improved skin-protecting characteristics
DE1277495,
DE2612095,
DE3011549,
GB797119,
NL7304068,
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Feb 17 1982KLISCH, STEPHEN C COLGATE-PALMOLIVE COMPANY, 300 PARK AVENUE, NEW YORK, 22, NEW YORK, 10022, A CORP OF DE ASSIGNMENT OF ASSIGNORS INTEREST 0044470699 pdf
Feb 17 1982LAI, KUO-YANNCOLGATE-PALMOLIVE COMPANY, 300 PARK AVENUE, NEW YORK, 22, NEW YORK, 10022, A CORP OF DE ASSIGNMENT OF ASSIGNORS INTEREST 0044470699 pdf
Feb 17 1982ROBBINS, CLARENCE R COLGATE-PALMOLIVE COMPANY, 300 PARK AVENUE, NEW YORK, 22, NEW YORK, 10022, A CORP OF DE ASSIGNMENT OF ASSIGNORS INTEREST 0044470699 pdf
Feb 19 1982Colgate-Palmolive Company(assignment on the face of the patent)
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